Xueyan Wu

Peking Union Medical College Hospital

H指数:11

被引数:528

个人简介

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EP1782 - LBA_ECE_1381 - Short- and long-term effects of hormonal replacement on body composition and metabolism in congenital hypogonadotropic hypogonadism—a study combining longitudinal and cross-sectional cohorts

EP1782 - LBA_ECE_1381 - 激素替代治疗对先天性低促性腺激素性性腺功能减退症患者体成分和代谢的短期和长期影响——一项结合纵向和横断面队列的研究

European Journal of Endocrinology

IF5.2

2026-08-100

OAAI

Metabolic and reproductive roles of irisin in polycystic ovary syndrome: from mechanistic insights to therapeutic perspectives

在多囊卵巢综合征中irisin的代谢与生殖作用：从机制洞察到治疗前景

Diabetes Research and Clinical Practice

IF7.4

2025-12-010

PRE

Sperm DNA methylation profiling in patients with Kallmann syndrome

Kallmann综合征患者精子DNA甲基化谱分析

ENDOCRINE CONNECTIONS

IF2.8

2025-10-010

PRE

The Efficacy of Semaglutide on Hypothalamic Obesity Caused by Craniopharyngioma Surgery

Semaglutide对颅咽管瘤手术引起的下丘脑肥胖的疗效

Clinical Endocrinology

IF2.4

2025-05-270

PRE

Hyperprolactinemia Is Associated With Height Attainment Within or Above Target Height in Adult Patients With Pituitary Stalk Interruption Syndrome

高泌乳素血症与垂体柄中断综合征成年患者靶身高内或超出靶身高的身高达成相关。

Endocrine Practice

IF4.6

2025-03-250

PRE

Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation

通过长读测序和表型相关性检测到的21-羟化酶缺乏症中的嵌合CYP21A1P/CYP21A2基因

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2025-02-040

Mechanism of female CHH caused by compound heterozygous mutations in the LHB gene

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2025-01-090

PRE

Body Composition, Adipocytokine, and Metabolic Parameters in Men With Congenital Hypogonadotropic Hypogonadism

先天性低促性腺激素性性腺功能减退症男性的身体成分，脂肪细胞因子和代谢参数

CLINICAL ENDOCRINOLOGY

IF2.4

2025-01-050

PRE

CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2024-06-272

Clinical manifestations and spermatogenesis outcomes in Chinese patients with congenital hypogonadotropic hypogonadism caused by inherited or de novo FGFR1 mutations

ASIAN JOURNAL OF ANDROLOGY

IF2.7

2024-01-091

OAAI

The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development

中国一系列46，XY性发育障碍患者的遗传谱

ANDROLOGY

IF3.4

2023-05-1911

PRE

Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism (vol 9, e14779, 2023)

HELIYON

IF3.6

2023-05-010

OAAI

Molecular analysis of 12 Chinese patients with 11β-hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants

FASEB JOURNAL

IF4.2

2023-03-172

PRE

The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant

携带P31L变体的21-羟化酶缺乏症患者的简单男性化表型的根本原因

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-02-140

OAAI

Pharmacological effects of salidroside on central nervous system diseases

BIOMEDICINE & PHARMACOTHERAPY

IF7.5

2022-12-0125

PRE

Mutation of c.244G>T in NR5A1 gene causing 46, XY DSD by affecting RNA splicing

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-08-303

OAAI

Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients

CLINICAL ENDOCRINOLOGY

IF2.4

2021-04-309

PREAI

Bone mineral density and trabecular bone score in patients with 21-hydroxylase deficiency after glucocorticoid treatment

CLINICAL ENDOCRINOLOGY

IF2.4

2021-03-077

PREAI

AROMATASE INHIBITOR INCREASES THE HEIGHT OF PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

ENDOCRINE PRACTICE

IF4.6

2020-09-018

PRE

The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2020-04-1523

OAAI

Xueyan Wu

个人简介

教育背景

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